Electronic personal health records and systems to improve care for vulnerable populations

Association for Information Systems - 13th Americas Conference on Information Systems, AMCIS 2007: Reaching New Heights

Volumn 1, Issue , 2007, Pages 720-727

  Botts, Nathan E ^a  

^a CLAREMONT GRADUATE UNIVERSITY   (United States)

Author keywords

Patient centered care; Patient physician communication; Personal health records; Vulnerable populations

Indexed keywords

EVALUATION MEASURES; HEALTH AWARENESS; HEALTH CARE PROVIDERS; HEALTH INFORMATIONS; HEALTH SERVICES; PATIENT-CENTERED CARE; PERSONAL HEALTH RECORD; SELF MANAGEMENT; USABILITY FACTORS; VULNERABLE POPULATIONS;

COMMUNICATION; HEALTH; INFORMATION SYSTEMS;

HEALTH CARE;

EID: 84870161407     PISSN: None     EISSN: None     Source Type: Conference Proceeding    
DOI: None     Document Type: Conference Paper

References (16)

1. AHRQ. (2003). National Healthcare Disparities Report, 2003. Retrieved From http://www.ahrq.gov/qual/nhdr03/nhdr03.htm.
2. Bandura, A. (1997). Self Efficacy: The Exercise of Control. New York, N.Y.: WH Freeman Co.
3. Bergeson, S. C., & Dean, J. D. (2006). A Systems Approach to Patient-Centered Care. JAMA, 296(23), 2848-2851
4. Berland G., Elliot, M. N., Morales L.S., Algazy J.I., Kravitz R.L., Broder M.S., Kanouse D.E., Munoz J.A., Puyol J.A., Lara M., Watkins K.E., Yang H., McGlynn E.A. (2001). Health Information on the Internet: Accessibility, Quality, and Readability in English and Spanish. Journal of the American Medical Association, 285(20), 2612-2621.
5. Bodenheimer, T., Lorig, K., Holman, H., & Grumbach, K. (2002). Patient Self-management of Chronic Disease in Primary Care. JAMA, 288(19), 2469-2475.
6. Brooke, J. (Ed.). (1996). SUS: A Quick and Dirty Usability Scale. London: Taylor & Francis.
7. Conn, J. (2006). Feds could have bigger role in PHR push; health literacy a concern [Electronic Version]. ModernHealthCare.com. Retrieved 09/19/2006 from http://www.modernhealthcare.com/printwindow.cms?articleId=41578&pageType=article.
8. Greene, J., Yedidia, M.J. (2005). Provider Behaviors Contributing to Patient Self-Management of Chronic Illness Among Underserved Populations. Journal of Health Care for the Poor and Underserved 16(4), 808-824.
9. Group, P. H. W. (2003). Connecting for Health. New York, NY: Markle Foundation.
10. Kim, M. I., Johnson, K.B. (2002). Personal Health Records: Evaluation of Functionality and Utility. Journal of the American Medical Informatics Association, 9(2), 171-180.
11. Relman, A. (1985). Economic considerations in emergency care. The New England Journal of Medicine, 32(6), 372-373.
12. Rotter, J. (1982). The development and application of social learning theory. New York: Praeger Publishers.
13. Shesser, R., Kirsch, T., Smith, J., Hirsch, R. (1991). An analysis of emergency department use by patients with minor illness. Annals of Emergency Medicine, 20(7), 743-748.
14. Tang, P. C., Ash, J.S., Bates, D.W., Overhage, M., Sands, D.Z. (2006). Personal Health Records: Definitions, Benefits, and Strategies for Overcoming Barriers to Adoption. Journal of the American Medical Association, 13(2), 121-126.
15. Wallston, K. A., Wallston, B. S., Smith, S., & Dobbins, C. J. (1987). Perceived control and health. Current Psychological Research and Reviews, 6, 5-25.
16. Winkelman, W. J., Leonard, K.J., Rossos, P.G. (2005). Patient-Perceived Usefulness of Online Electronic Medical Records: Employing Grounded Theory in the Development of Information and Communication Technologies for Use by Patients Living with Chronic Illness. Journal of the American Medical Informatics Association, 12(3), 306-314.